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FDA 510(k), K131401, BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
FDA 510(k), K131401, BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
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510(K) Number: K131401
Device Name: BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
Manufacturer: MERCATOR MEDSYSTEMS, INC.
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 05/15/2013
Decision Date: 07/02/2013
Regulation Medical Specialty: Ear Nose & Throat
Device Name: BLOWFISH TRANSBRONCHIAL MICRO-INFUSION CATHETER
Manufacturer: MERCATOR MEDSYSTEMS, INC.
Device Classification Name: Bronchoscope (Flexible Or Rigid)
Regulation Number: 874.4680
Classification Product Code: EOQ
Date Received: 05/15/2013
Decision Date: 07/02/2013
Regulation Medical Specialty: Ear Nose & Throat
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- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
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